The individual has a responsibility to work with QC Scientists (QC SCi) and Laboratory supervisors where appropriate to conduct all work in compliance with applicable regulatory requirements, and specifically those regulations (GLP and or GCP / and or GMP) specified in the study plans, protocols, or work agreements governing the work in which they are involved, and ensure that client deadlines are met. They are also responsible for the efficient completion of laboratory procedures within BioPharmCMC.
To provide operational support necessary for the performance of a wide variety of studies carried out in BioPharmCMC, working with minimal supervision. Will work closely with Laboratory Supervisors and BioPharmCMC Management to ensure efficient and proper operation of area.
The post holder should typically have: